1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide
1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide
CAS: 884863-08-5
Molecular Formula: C22H22BrN
1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide - Names and Identifiers
| Name | 1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide |
| Synonyms | 1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide 1,2,3-Trimethyl-1-benzyl-1H-benzo[e]indolium bromide 1,2,3-trimethyl-3-(phenylmethyl)benzo[e]indol-3-ium bromide 1H-Benz[e]indolium, 1,2,3-trimethyl-1-(phenylmethyl)-, bromide |
| CAS | 884863-08-5 |
| InChI | InChI=1/C22H22N.BrH/c1-16-17(2)23(3,15-18-9-5-4-6-10-18)21-14-13-19-11-7-8-12-20(19)22(16)21;/h4-14H,15H2,1-3H3;1H/q+1;/p-1 |
1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide - Physico-chemical Properties
| Molecular Formula | C22H22BrN |
| Molar Mass | 380.32 |
1,2,3-Trimethyl-3-benzyl-3H-benz[e]indolium bromide - Introduction
1,2, [e]indolium bromide is an organic compound with a chemical formula of C24H23NBr and a structure containing 3 methyl groups and a benzyl group. It is a bromide salt whose cationic moiety is trimethylbenzylindole.
The compound has a solid crystalline form and is soluble in polar solvents such as water and alcohols. It has a molecular weight of 407.3g/mol.
1,2, [e]indolium bromide catalysts commonly used in chemical reactions. It can be used as a green synthesis reagent for a variety of reactions in organic synthesis, such as substitution reactions, coupling reactions and cyclization reactions. It can also be used for stains and fluorescent probes for metal ions and metal complexes.
The compound can be prepared by a synthetic reaction. A common method is to react benzindole with trimethylammonium bromide and benzyl bromide to generate 1,2, [e]indolium bromide.
When using and handling, attention should be paid to the safety of the compound. It can be irritating and allergic to the eyes and skin. Avoid ingestion, contact and inhalation during operation. When exposed to the compound, immediately flush the affected area with plenty of water and seek medical help. Relevant safety regulations and operating instructions shall be observed during storage and handling.
The compound has a solid crystalline form and is soluble in polar solvents such as water and alcohols. It has a molecular weight of 407.3g/mol.
1,2, [e]indolium bromide catalysts commonly used in chemical reactions. It can be used as a green synthesis reagent for a variety of reactions in organic synthesis, such as substitution reactions, coupling reactions and cyclization reactions. It can also be used for stains and fluorescent probes for metal ions and metal complexes.
The compound can be prepared by a synthetic reaction. A common method is to react benzindole with trimethylammonium bromide and benzyl bromide to generate 1,2, [e]indolium bromide.
When using and handling, attention should be paid to the safety of the compound. It can be irritating and allergic to the eyes and skin. Avoid ingestion, contact and inhalation during operation. When exposed to the compound, immediately flush the affected area with plenty of water and seek medical help. Relevant safety regulations and operating instructions shall be observed during storage and handling.
Last Update：2024-04-10 22:29:15
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